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Analysis of antibody reactivity against cysteine sulfinic acid decarboxylase, a pyridoxal phosphate-dependent enzyme, in endocrine autoimmune disease

Sköldberg, Filip (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Autoimmuna sjukdomar (Kämpe)
Rorsman, Fredrik (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Autoimmuna sjukdomar (Kämpe)
Perheentupa, Jaakko (author)
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Landin-Olsson, Mona (author)
Lund University,Lunds universitet,Medicin, Lund,Sektion II,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Medicine, Lund,Section II,Department of Clinical Sciences, Lund,Faculty of Medicine
Husebye, Eystein S. (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Autoimmuna sjukdomar (Kämpe)
Gustafsson, Jan (author)
Barnendokrinologisk forskning/Tuvemo
Kämpe, Olle (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Autoimmuna sjukdomar (Kämpe)
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 (creator_code:org_t)
The Endocrine Society, 2004
2004
English.
In: Journal of Clinical Endocrinology and Metabolism. - : The Endocrine Society. - 0021-972X .- 1945-7197. ; 89:4, s. 1636-1640
  • Journal article (other academic/artistic)
Abstract Subject headings
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  • The structurally related group II pyridoxal phosphate (PLP)-dependent amino acid decarboxylases glutamic acid decarboxylase (GAD), aromatic L-amino acid decarboxylase (AADC), and histidine decarboxylase (HDC) are known autoantigens in endocrine disorders. We report, for the first time, the prevalence of serum autoantibody reactivity against cysteine sulfinic acid decarboxylase (CSAD), an enzyme that shares 50% amino acid identity with the 65- and 67-kDa isoforms of GAD (GAD-65 and GAD-67), in endocrine autoimmune disease. Three of 83 patients (3.6%) with autoimmune polyendocrine syndrome type 1 (APS1) were anti-CSAD positive in a radioimmunoprecipitation assay. Anti-CSAD antibodies cross-reacted with GAD-65, and the anti-CSAD-positive sera were also reactive with AADC and HDC. The low frequency of anti-CSAD reactivity is in striking contrast to the prevalence of antibodies against GAD-65, AADC, and HDC in APS1 patients, suggesting that different mechanisms control the immunological tolerance toward CSAD and the other group II decarboxylases. Moreover, CSAD may be a useful mold for the construction of recombinant chimerical antigens in attempts to map conformational epitopes on other group II PLP-dependent amino acid decarboxylases.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Annan klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Other Clinical Medicine (hsv//eng)

Keyword

Addison Disease/immunology
Aromatic-L-Amino-Acid Decarboxylases/immunology
Autoantibodies/*blood/immunology
Carboxy-Lyases/*immunology
Cross Reactions
Diabetes Mellitus; Type 1/immunology
Female
Glutamate Decarboxylase/immunology
Histidine Decarboxylase/immunology
Humans
Isoenzymes/immunology
Male
Polyendocrinopathies; Autoimmune/*immunology
Pyridoxal Phosphate/metabolism
Radioimmunoprecipitation Assay
Research Support; Non-U.S. Gov't
MEDICINE
MEDICIN

Publication and Content Type

vet (subject category)
art (subject category)

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